New Jersey recalls
3,688 federal recalls affecting New Jersey in the last 12 months - 340 New Jersey-specific plus 3,348 nationwide. Sourced from CPSC, FDA, USDA, and NHTSA.
- 2026-07-01FDA-FoodSpring & MulberryClass INationwideSpring & Mulberry chocolate recalled for Salmonella risk
Spring & Mulberry Lavender Rose Date-Sweetened Chocolate bars may be contaminated with Salmonella. The recall affects specific batch lots with use-by dates ranging from January through August 2027. No illnesses have been reported.
- 2026-07-01FDA-FoodSpring & MulberryClass INationwideSpring & Mulberry chocolate recalled for Salmonella risk
Spring & Mulberry Earl Grey Date-Sweetened Chocolate bars may be contaminated with Salmonella. The affected product is a 2.1 oz. chocolate bar in a purple box sold individually and in multi-packs on Amazon, with specific lot numbers and use-by dates identified.
- 2026-07-01FDA-FoodSpring & MulberryClass INationwideSpring & Mulberry chocolate bars recalled for Salmonella risk
Spring & Mulberry Mixed Berry Date-Sweetened Chocolate bars (2.1 oz) may be contaminated with Salmonella. The affected product was distributed nationwide and sold individually and in multi-packs on Amazon. Salmonella can cause serious illness.
- 2026-07-01FDA-FoodSpring & MulberryClass INationwideSpring & Mulberry Mint Leaf Date-Sweetened Chocolate, Net Wt. 2.1 oz. (60g), individually packaged in a teal green cardboard box, UPC 850055470217, Dist. By Spring & Mulberry Raleigh, NC 27606. Wholesale product packed 48 bars (caddied)/56 bars (uncaddied) per case. Retail product sold individually or as a 3-pk, 6-pk, or 12-pk (Amazon only).
Potential Salmonella contamination
- 2026-07-01FDA-FoodChampion FoodsClass IINationwideMotor City Pizza Co. 5 Cheese Bread recalled for Salmonella risk
Motor City Pizza Co. 5 Cheese Bread products may contain Salmonella, a bacteria that can cause serious illness. The affected products were distributed nationwide to major retailers including Costco, Walmart, Target, and Kroger.
- 2026-07-01FDA-FoodJoy GourmetClass IIJoy Saffron Cardamom Lassi recalled for inadequate pasteurization
Joy Gourmet Foods LLC recalled Saffron Cardamom Lassi (16 oz bottles) because the product was not adequately pasteurized, which means it may not have been heated sufficiently to kill harmful bacteria. The affected bottles have expiration dates between June 30 and July 30, 2026, and were distributed in New York, New Jersey, and Pennsylvania.
- 2026-07-01FDA-FoodJoy Gourmet FoodsClass IIJoy Orange Lassi recalled for inadequate pasteurization
Joy Gourmet Foods LLC is recalling 16 oz. bottles of Joy Orange Lassi due to inadequate pasteurization, which may allow harmful bacteria to grow. The affected product was distributed in New York, New Jersey, and Pennsylvania with expiration dates between June 30 and July 30, 2026.
- 2026-07-01FDA-FoodJoy Gourmet FoodsClass IIJoy Peach Lassi recalled for inadequate pasteurization
Joy Gourmet Foods' Peach Lassi beverage was not pasteurized to the required temperature, which means harmful bacteria may not have been eliminated. The affected product was distributed in New York, New Jersey, and Pennsylvania with expiration dates between June 30 and July 30, 2026.
- 2026-07-01FDA-FoodJoy Gourmet FoodsClass IIJoy Gourmet Foods Mint Lassi recalled for pasteurization issue
Joy Gourmet Foods Mint Lassi 16 oz. was not adequately pasteurized during production. The affected product has expiration dates between June 30 and July 30, 2026 and was distributed in New York, New Jersey, and Pennsylvania.
- 2026-07-01FDA-FoodJoy Gourmet FoodsClass IIJoy Gourmet Foods Masala Chaash Lassi recalled for pasteurization risk
Joy Gourmet Foods LLC is recalling Masala Chaash Lassi in 16 oz. and 64 oz. bottles because the product was not adequately pasteurized. Unpasteurized dairy products can contain harmful bacteria that may cause illness. The affected bottles have expiration dates between June 30 and July 30, 2026.
- 2026-07-01FDA-FoodJoy GourmetClass IIJoy Plain Chaash Lassi recalled for inadequate pasteurization
Joy Gourmet Foods LLC is recalling Plain Chaash Lassi in 16 oz. and 64 oz. bottles because the product was not adequately pasteurized, which means it may contain harmful bacteria. The affected products have expiration dates between June 30 and July 30, 2026, and were distributed in New York, New Jersey, and Pennsylvania.
- 2026-07-01FDA-FoodJoy Gourmet FoodsClass IIJoy Mango-Pina-Orange Lassi recalled for inadequate pasteurization
Joy Gourmet Foods LLC is recalling Mango-Pina-Orange Lassi in 16 oz. and 64 oz. bottles because the product was not adequately pasteurized. Inadequate pasteurization can allow harmful bacteria to survive in the beverage.
- 2026-07-01FDA-FoodJoy Gourmet FoodsClass IIJoy Gourmet Mango-Pina-Strawberry Lassi recalled for pasteurization risk
Joy Gourmet Foods' Mango-Pina-Strawberry Lassi (16 oz bottles) was not adequately pasteurized during production. Inadequate pasteurization can allow harmful bacteria to survive, posing a food safety risk. The affected product has expiration dates between June 30 and July 30, 2026, and was distributed in New York, New Jersey, and Pennsylvania.
- 2026-07-01FDA-FoodJoy Gourmet FoodsClass IIJoy Strawberry Lassi recalled for inadequate pasteurization
Joy Strawberry Lassi 16 oz. bottles were not adequately pasteurized, which means they may not have been heated sufficiently to kill harmful bacteria. The affected product was distributed in New York, New Jersey, and Pennsylvania, with expiration dates between June 30 and July 30, 2026.
- 2026-07-01FDA-FoodJoy Gourmet FoodsClass IIJoy Pineapple Lassi recalled for inadequate pasteurization
Joy Gourmet Foods LLC recalled 16 oz bottles of Joy Pineapple Lassi because the product was not adequately pasteurized. This means harmful bacteria may not have been fully eliminated during processing. The affected bottles were distributed in New York, New Jersey, and Pennsylvania with expiration dates between June 30 and July 30, 2026.
- 2026-07-01FDA-FoodJoy Gourmet FoodsClass IIJoy Gourmet Foods salty lassi recalled for pasteurization risk
Joy Gourmet Foods LLC's 16 oz. salty lassi product was not adequately pasteurized during production. The affected bottles have expiration dates between June 30 and July 30, 2026. No illnesses have been reported.
- 2026-07-01FDA-FoodJoy Gourmet FoodsClass IIJoy Gourmet Foods Sweet Lassi recalled for pasteurization risk
Joy Gourmet Foods Sweet Lassi 16 oz. was not adequately pasteurized, which means it may contain harmful bacteria. The affected product has expiration dates between June 30 and July 30, 2026, and was distributed in New York, New Jersey, and Pennsylvania.
- 2026-07-01FDA-FoodJoy Gourmet FoodsClass IIJoy Rose Lassi recalled for inadequate pasteurization
Joy Gourmet Foods' Rose Lassi drink (16 oz bottles) was not adequately pasteurized during production. This means harmful bacteria may not have been fully eliminated. The affected product was distributed in New York, New Jersey, and Pennsylvania, with expiration dates between June 30 and July 30, 2026.
- 2026-07-01FDA-FoodJoy Gourmet FoodsClass IIJoy Mango Lassi recalled for inadequate pasteurization
Joy Gourmet Foods' mango lassi (16 oz. and 64 oz. bottles) was not adequately pasteurized during manufacturing. Inadequate pasteurization can allow harmful bacteria to survive in the product. Affected bottles have expiration dates between June 30 and July 30, 2026.
- 2026-07-01FDA-DrugSun PharmaceuticalClass IINationwideSun Pharmaceutical Perampanel recalled for tablet strength mix-up
Sun Pharmaceutical discovered that some bottles labeled as containing 6mg Perampanel tablets actually contained 10mg tablets instead. This mix-up affects one lot (AE01763) distributed nationwide. Patients taking the wrong strength could receive an incorrect dose of this seizure medication.
- 2026-07-01FDA-DrugElevate Oral CareClass IINationwideElevate Oral Care Povi-One recalled for sub-potency
Elevate Oral Care's Povi-One 10% Povidone-Iodine Oral Antiseptic does not contain the full strength stated on the label. Five specific production lots distributed nationwide do not meet the required potency standard, which means the product may not work as intended for oral antiseptic purposes.
- 2026-07-01FDA-DrugAnnora PharmaClass IINationwideCamber Lacosamide tablets recalled for Selexipag mix-up
Some bottles of Lacosamide 100mg tablets may contain Selexipag 1000 mcg tablets instead. This mix-up happened during manufacturing and could cause patients to take the wrong medication. The recall affects specific lots distributed nationwide.
- 2026-07-01FDA-DrugCareFusionClass INationwideBD ChloraPrep FREPP Clear recalled for sterility concerns
BD ChloraPrep FREPP Clear, a sterile skin antiseptic applicator, may contain fungal contamination (Aspergillus penicillioides) or may not be fully sterile due to wrinkles in the packaging seal. Approximately 178,000 applicators from lot 4073005 (expiring 03/31/2027) are affected nationwide and internationally.
- 2026-07-01FDA-DrugCareFusionClass INationwideBD ChloraPrep Clear recalled for fungal contamination risk
BD ChloraPrep Clear, a sterile antiseptic skin-prep solution used before medical procedures, was found to contain Aspergillus penicillioides fungus in some applicators. This affects the sterility of the product, which is critical for medical use. The affected lot is Lot #4032183 with an expiration date of January 31, 2027.
- 2026-07-01FDA-DrugCareFusionClass IINationwideBD ChloraPrep FREPP Clear recalled for sterility risk
BD ChloraPrep FREPP Clear applicators may have wrinkles in the paper lid that could compromise the sterile seal. This affects multiple lot numbers distributed nationwide through mid-2027. No injuries have been reported.
- 2026-07-01FDA-DrugCareFusionClass IINationwideBD ChloraPrep Clear recalled for sterility assurance concern
BD ChloraPrep Clear, a sterile skin antiseptic solution used before medical procedures, is being recalled because wrinkles in the paper packaging lid may allow the sterile seal to be breached. This defect could potentially allow contamination of the product. No injuries have been reported.
- 2026-07-01FDA-DrugANI PharmaceuticalsClass IIINationwideANI Pharmaceuticals hydroxyzine solution recalled for foreign substance
ANI Pharmaceuticals is recalling hydroxyzine hydrochloride oral solution (10 mg/5 mL, 473 mL bottles) due to the presence of a foreign substance in one lot. The affected product was distributed nationwide. No injuries have been reported.
- 2026-07-01FDA-DrugDirect RxClass IINationwideDirect Rx Duloxetine D/R recalled for impurity risk
Direct Rx's packaged Duloxetine D/R 30 mg capsules contain levels of N-nitroso-duloxetine, a potentially harmful impurity, above FDA's recommended limit. This is a manufacturing quality issue affecting specific lots distributed nationwide.
- 2026-07-01FDA-DrugAmgenClass IINationwideAmgen Sensipar cinacalcet tablets recalled for manufacturing deviations
Amgen is recalling Sensipar (cinacalcet) 90mg tablets due to deviations from current good manufacturing practice (CGMP) standards. This affects one lot distributed nationwide. No injuries have been reported.
- 2026-07-01FDA-DrugAmgenClass IINationwideAmgen Corlanor recalled for foreign substance contamination
Amgen is recalling specific lots of Corlanor (ivabradine) 7.5mg tablets due to the presence of a foreign substance in some bottles. The affected lots were distributed nationwide. No injuries have been reported.
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